Screening for Intracranial Aneurysms in Elderly Males with Family History
Yes, screening with MRA or CTA is recommended for an elderly male with a family history of intracranial aneurysm, particularly if there are two or more affected first-degree relatives. 1, 2
Risk Stratification Based on Family History
The strength of your screening recommendation depends on the number of affected relatives:
Two or more first-degree relatives with aneurysm or SAH: Screening is strongly recommended (Class I; Level of Evidence B), as this defines familial intracranial aneurysm syndrome with approximately 8% risk of harboring an unruptured aneurysm 1, 2
One first-degree relative with aneurysm: Screening should be offered, especially with additional risk factors (hypertension, smoking, female sex), as the relative risk is 4.2 compared to the general population 1, 2
General population without family history: Screening is not recommended, as it is not cost-effective and may cause more harm than benefit 1
Additional Risk Factors That Strengthen Screening Indication
Beyond family history, these factors increase the likelihood of detecting an aneurysm and should prompt screening even with only one affected relative 2, 3:
- Current or former cigarette smoking
- History of hypertension
- Female sex
- Higher lipid levels
- Elevated fasting glucose
Recommended Imaging Modality
MRA without contrast is the preferred initial screening method 1, 2, 3:
- Sensitivity: 69-93% for aneurysms >3-5 mm 1, 2
- Specificity: 89% 3
- Non-invasive with no radiation exposure, making it ideal for screening 2, 3
CT angiography is an acceptable alternative 1, 2:
- Sensitivity: 77-97% for aneurysms as small as 2-3 mm 1, 2
- Involves radiation exposure, less ideal for repeated screening 3
Catheter angiography remains the gold standard but should be reserved for symptomatic patients or when MRA/CTA findings are equivocal, given its invasive nature and <0.5% permanent neurological morbidity risk 1, 4
Screening Frequency and Duration
Screen every 5-7 years from age 20 to 80 years if two or more first-degree relatives are affected 3, 5:
- Long-term data shows aneurysms detected in 11% at first screening, 8% at second screening, 5% at third screening, and 5% at fourth screening 5
- The yield remains substantial even after two negative screens, with 3% developing de-novo aneurysms 5
- One patient developed a ruptured aneurysm 3 years after a negative screen, suggesting intervals may need to be shorter in some cases 5, 6
For elderly males specifically: Continue screening until age 65-80 years, as life expectancy and competing health risks must be considered 3
Critical Risk Factor Modification
Regardless of screening results, aggressively address modifiable risk factors 2, 3:
- Smoking cessation is critical: Smoking is one of the strongest modifiable risk factors for both aneurysm formation and rupture 2, 3
- Blood pressure control: Reducing diastolic blood pressure by 6 mmHg produces a 42% reduction in stroke incidence 3
- Avoid sympathomimetic drugs: Including cocaine and phenylpropanolamine 3
- Limit alcohol consumption: Heavy use is an independent risk factor for SAH 3
Important Caveats
The family member's aneurysm causing diplopia suggests a symptomatic lesion, which is clinically significant 4:
- Symptomatic aneurysms causing mass effect (like cranial nerve palsies with diplopia) warrant urgent neurosurgical evaluation and strong consideration for treatment regardless of size 4
- This distinguishes it from asymptomatic screening scenarios and suggests higher risk 4
Screening is not without risks 7:
- One older study suggested screening 1000 individuals three times resulted in poor outcomes in 14 patients (from screening/treatment complications) versus 15 without screening, questioning cost-effectiveness 7
- However, this 1999 study used older imaging and surgical techniques; modern data from 2014 shows substantial yield with serial screening 5
If an aneurysm is detected, treatment decisions must consider 1, 4:
- Patient age and life expectancy
- Aneurysm size (rupture risk increases significantly with size >7mm) 1
- Location (posterior circulation and posterior communicating artery have higher rupture risk) 1
- Morphology (irregular shape, daughter sacs increase rupture risk) 4
- Symptomatic versus asymptomatic presentation 4
Special genetic conditions warrant screening even without family history 2, 3: